The phrase "active catalysis" is correct and usable in written English.
It can be used in scientific contexts, particularly in chemistry or biochemistry, to describe a process where a catalyst is actively facilitating a reaction.
Example: "The study focused on the mechanisms of active catalysis in enzyme reactions, highlighting the importance of substrate binding."
Alternatives: "catalytic activity" or "catalyst action".
When using molecular aggregates as a catalyst, the efficient catalysis via an multi-electron transfer reduction by the complex often takes place coupled with the intrinsic characteristics of the polymer employed; moreover, they show unique and active catalysis that cannot be achieved by the corresponding neat complex in a solution or in an electrode-coated state.
Importantly, catalytically inhibited Zap70 can still participate in signal transduction without active catalysis, by interacting with other signalling proteins via its phosphorylated tyrosines.
Alternatively, binding of ATP to noncatalytic nucleotide binding sites (hosted primarily by an α-subunit) may be required for fully active catalysis (18), and this binding may be slow at low temperatures.
Upon binding of activators, the catalytic P-loop changes its conformation to allow the catalytic cysteine and arginine residues to be positioned in its proximity as seen in other active PI phosphatases, such as PTEN, leading to active catalysis.
Upon activation with oxygen sites of the form [Fe(III 2 μ-η1:η1-O2)(HPTP ]4+ (1) and [Fe(IV 2 O 2 HPTP ]4+ (2) appear to be active in catalysis.
Specifically, if you are from an interdisciplinary related area and naturally not too familiar with all vocabulary used in the field, you will find it particulary useful to have this encyclopedia on your bookshelf". --Jorg Libuda, Fritz-Haber-Institut der Max-Planck-Gesellschaft, Berlin, ChemPhysChem "...this book is a must for all libraries in institutes with research groups active in catalysis.
In this context, the edges and corners of ZnOE hexagonal particles have many coordinatively unsaturated sites, which usually are active in catalysis.
This hydroxyl is not acidic (or at least not active in catalysis), as it resides in the sodalite cages.
Chelation of metal ion is the main strategy to avoid ROS generation that is associated with redox active metal catalysis [ 10, 39].
The main strategy to avoid ROS generation that is associated with redox active metal catalysis involves chelation of the metal ions [ 47, 48].
These sensors were employed to assess the effect of simultaneous multiple active site catalysis on the kinetic properties of the individual subunits.
